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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257524Generated: November 2, 2026

Methanol → Tert-butyl 3-bromo-5-(hydroxymethyl)benzoate

https://huagongshe.com/reaction/1257524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantTert-butyl methyl 5-bromoisophthalateHCID 66896065—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-bromo-5-(hydroxymethyl)benzoateHCID 5809619181.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl methyl 5-bromoisophthalate (3.63 g, 11.5 mmol) in tetrahydrofuran (90 mL) at 0° C. was added portionwise sodium borohydride (1.53 g, 40.3 mmol). The mixture was stirred at 0° C. After 30 min, methanol (4.2 mL, 92.0 mmol) was added and the mixture was heated to 40° C. After 6 h, the mixture was cooled to ambient temperature and the mixture was quenched with methanol and concentrated. Ethyl acetate was added and the mixture was washed with brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→50% hexanes/ethyl acetate) gave the title compound (2.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461185B2
Source datasetuspto-grants-2013_06
ORD IDord-58805491a88f4125a5c9b26f9c6f4aec
Source noteuspto-grants-2013_06